chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91212866	91212867	C	A	6	GENIC	homozygous	51539279
10	91212981	91212982	C	T	10	GENIC	homozygous	52575027
10	91213312	91213313	G	A	12	GENIC	possibly homozygous	52575029
10	91215806	91215807	C	-	5	GENIC	heterozygous	51539280
10	91216360	91216361	G	A	20	GENIC	possibly homozygous	51539282
10	91218114	91218115	G	-	3	INTERGENIC	heterozygous	51739182
10	91219593	91219594	T	C	20	GENIC	possibly homozygous	52575031
10	91219687	91219688	G	T	22	GENIC	possibly homozygous	51539284
10	91219732	91219733	T	TC	29	GENIC	homozygous	52575033
10	91221084	91221085	G	A	12	GENIC	heterozygous	51539288
10	91221477	91221478	C	G	23	GENIC	possibly homozygous	51539293
10	91221580	91221581	C	T	18	GENIC	possibly homozygous	51539294
10	91221634	91221635	A	G	18	GENIC	heterozygous	51539295
10	91222132	91222133	G	A	26	GENIC	possibly homozygous	51539296